Defining the T cell antigen proteome of wasp venom

Clin Exp Allergy. 2006 Oct;36(10):1274-80. doi: 10.1111/j.1365-2222.2006.02569.x.

Abstract

Background: While modulation of T cell function is believed to be important in the successful acquisition of clinical tolerance during venom immunotherapy, little is known of the role of wasp venom specific T cell antigens.

Objective: We sought comprehensively to characterize the T cell proteome for wasp venom to facilitate the future development of T cell-based immunotherapeutic approaches.

Methods: Using peripheral blood mononuclear cells from wasp venom-allergic individuals and IL-4 ELISPOT analysis, we characterized T cell responses to whole venom and gel filtration/ion exchange-fractionated venom. Reactive fractions were purified and identified using highly sensitive electrospray ion-trap mass spectrometry.

Results: Wasp venom-allergic individuals have detectable whole wasp venom-specific T cells directly ex vivo, which show rapid IL-4 effector function. T cell responses to gel filtration/ion exchange fractionated venom were dominated by responses to phospholipase A(1), hyaluronidase and antigen 5.

Conclusion: Although it is likely that there are many T cell antigens within wasp venom, the main responses are to proteins coincident with the known IgE-binding proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Antigens / genetics*
  • Case-Control Studies
  • Chromatography, Gel
  • Chromatography, Ion Exchange
  • Desensitization, Immunologic
  • Female
  • Humans
  • Hyaluronoglucosaminidase / analysis
  • Hypersensitivity, Immediate / immunology
  • Interleukin-4 / immunology
  • Male
  • Middle Aged
  • Phospholipases / analysis
  • Proteome*
  • Receptors, IgE / analysis
  • Spectrometry, Mass, Electrospray Ionization
  • T-Lymphocytes / immunology*
  • Wasp Venoms / analysis
  • Wasp Venoms / immunology*

Substances

  • Antigens
  • Proteome
  • Receptors, IgE
  • Wasp Venoms
  • white-faced hornet venom antigen 5
  • Interleukin-4
  • Phospholipases
  • Hyaluronoglucosaminidase